Porphyrins. 29. Mass spectra of functionally substituted tetraarylporphyrin derivatives View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1993-12

AUTHORS

I. M. Karnaukh, A. S. Moskovskin, G. V. Ponomarev

ABSTRACT

The mass spectral behavior of functionally substituted meso(p-adamantylphenyl)triphenylporphyrins and their p-methoxy-substituted analogs was studied. Breakdown of the M+ ions of these compounds proceeds chiefly-with a loss of the functional substituent in the adamantane ring with the formation of ions, which make it possible to determine the nature of this substituent.

PAGES

1418-1420

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00531403

DOI

http://dx.doi.org/10.1007/bf00531403

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1010866494


Indexing Status Check whether this publication has been indexed by Scopus and Web Of Science using the SN Indexing Status Tool
Incoming Citations Browse incoming citations for this publication using opencitations.net

JSON-LD is the canonical representation for SciGraph data.

TIP: You can open this SciGraph record using an external JSON-LD service: JSON-LD Playground Google SDTT

[
  {
    "@context": "https://springernature.github.io/scigraph/jsonld/sgcontext.json", 
    "about": [
      {
        "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/03", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Chemical Sciences", 
        "type": "DefinedTerm"
      }, 
      {
        "id": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/0305", 
        "inDefinedTermSet": "http://purl.org/au-research/vocabulary/anzsrc-for/2008/", 
        "name": "Organic Chemistry", 
        "type": "DefinedTerm"
      }
    ], 
    "author": [
      {
        "affiliation": {
          "alternateName": "Zashchita Specialized Center for Emergency Medical Aid, Ministry of Health of Russia, 123182, Moscow", 
          "id": "http://www.grid.ac/institutes/grid.415738.c", 
          "name": [
            "Zashchita Specialized Center for Emergency Medical Aid, Ministry of Health of Russia, 123182, Moscow"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Karnaukh", 
        "givenName": "I. M.", 
        "id": "sg:person.011451527031.71", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011451527031.71"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Zashchita Specialized Center for Emergency Medical Aid, Ministry of Health of Russia, 123182, Moscow", 
          "id": "http://www.grid.ac/institutes/grid.415738.c", 
          "name": [
            "Zashchita Specialized Center for Emergency Medical Aid, Ministry of Health of Russia, 123182, Moscow"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Moskovskin", 
        "givenName": "A. S.", 
        "id": "sg:person.012271247736.49", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012271247736.49"
        ], 
        "type": "Person"
      }, 
      {
        "affiliation": {
          "alternateName": "Zashchita Specialized Center for Emergency Medical Aid, Ministry of Health of Russia, 123182, Moscow", 
          "id": "http://www.grid.ac/institutes/grid.415738.c", 
          "name": [
            "Zashchita Specialized Center for Emergency Medical Aid, Ministry of Health of Russia, 123182, Moscow"
          ], 
          "type": "Organization"
        }, 
        "familyName": "Ponomarev", 
        "givenName": "G. V.", 
        "id": "sg:person.01070465134.19", 
        "sameAs": [
          "https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01070465134.19"
        ], 
        "type": "Person"
      }
    ], 
    "datePublished": "1993-12", 
    "datePublishedReg": "1993-12-01", 
    "description": "The mass spectral behavior of functionally substituted meso(p-adamantylphenyl)triphenylporphyrins and their p-methoxy-substituted analogs was studied. Breakdown of the M+ ions of these compounds proceeds chiefly-with a loss of the functional substituent in the adamantane ring with the formation of ions, which make it possible to determine the nature of this substituent.", 
    "genre": "article", 
    "id": "sg:pub.10.1007/bf00531403", 
    "inLanguage": "en", 
    "isAccessibleForFree": false, 
    "isPartOf": [
      {
        "id": "sg:journal.1358699", 
        "issn": [
          "0132-6244", 
          "1573-8353"
        ], 
        "name": "Chemistry of Heterocyclic Compounds", 
        "publisher": "Springer Nature", 
        "type": "Periodical"
      }, 
      {
        "issueNumber": "12", 
        "type": "PublicationIssue"
      }, 
      {
        "type": "PublicationVolume", 
        "volumeNumber": "29"
      }
    ], 
    "keywords": [
      "adamantane ring", 
      "methoxy-substituted analogs", 
      "loss", 
      "analogues", 
      "breakdown", 
      "compounds", 
      "formation", 
      "derivatives", 
      "behavior", 
      "nature", 
      "ring", 
      "substituents", 
      "spectra", 
      "ions", 
      "mass spectra", 
      "mass spectral behavior", 
      "functional substituents", 
      "spectral behavior", 
      "formation of ions", 
      "tetraarylporphyrin derivatives"
    ], 
    "name": "Porphyrins. 29. Mass spectra of functionally substituted tetraarylporphyrin derivatives", 
    "pagination": "1418-1420", 
    "productId": [
      {
        "name": "dimensions_id", 
        "type": "PropertyValue", 
        "value": [
          "pub.1010866494"
        ]
      }, 
      {
        "name": "doi", 
        "type": "PropertyValue", 
        "value": [
          "10.1007/bf00531403"
        ]
      }
    ], 
    "sameAs": [
      "https://doi.org/10.1007/bf00531403", 
      "https://app.dimensions.ai/details/publication/pub.1010866494"
    ], 
    "sdDataset": "articles", 
    "sdDatePublished": "2021-11-01T17:58", 
    "sdLicense": "https://scigraph.springernature.com/explorer/license/", 
    "sdPublisher": {
      "name": "Springer Nature - SN SciGraph project", 
      "type": "Organization"
    }, 
    "sdSource": "s3://com-springernature-scigraph/baseset/20211101/entities/gbq_results/article/article_223.jsonl", 
    "type": "ScholarlyArticle", 
    "url": "https://doi.org/10.1007/bf00531403"
  }
]
 

Download the RDF metadata as:  json-ld nt turtle xml License info

HOW TO GET THIS DATA PROGRAMMATICALLY:

JSON-LD is a popular format for linked data which is fully compatible with JSON.

curl -H 'Accept: application/ld+json' 'https://scigraph.springernature.com/pub.10.1007/bf00531403'

N-Triples is a line-based linked data format ideal for batch operations.

curl -H 'Accept: application/n-triples' 'https://scigraph.springernature.com/pub.10.1007/bf00531403'

Turtle is a human-readable linked data format.

curl -H 'Accept: text/turtle' 'https://scigraph.springernature.com/pub.10.1007/bf00531403'

RDF/XML is a standard XML format for linked data.

curl -H 'Accept: application/rdf+xml' 'https://scigraph.springernature.com/pub.10.1007/bf00531403'


 

This table displays all metadata directly associated to this object as RDF triples.

92 TRIPLES      21 PREDICATES      46 URIs      38 LITERALS      6 BLANK NODES

Subject Predicate Object
1 sg:pub.10.1007/bf00531403 schema:about anzsrc-for:03
2 anzsrc-for:0305
3 schema:author Nc57dd76277864514bbbf40d022c4ac5e
4 schema:datePublished 1993-12
5 schema:datePublishedReg 1993-12-01
6 schema:description The mass spectral behavior of functionally substituted meso(p-adamantylphenyl)triphenylporphyrins and their p-methoxy-substituted analogs was studied. Breakdown of the M+ ions of these compounds proceeds chiefly-with a loss of the functional substituent in the adamantane ring with the formation of ions, which make it possible to determine the nature of this substituent.
7 schema:genre article
8 schema:inLanguage en
9 schema:isAccessibleForFree false
10 schema:isPartOf N09fb4daf437b4efeb8cfba62b5fd81f4
11 Nb83273e3d4d749219a050483d0dded83
12 sg:journal.1358699
13 schema:keywords adamantane ring
14 analogues
15 behavior
16 breakdown
17 compounds
18 derivatives
19 formation
20 formation of ions
21 functional substituents
22 ions
23 loss
24 mass spectra
25 mass spectral behavior
26 methoxy-substituted analogs
27 nature
28 ring
29 spectra
30 spectral behavior
31 substituents
32 tetraarylporphyrin derivatives
33 schema:name Porphyrins. 29. Mass spectra of functionally substituted tetraarylporphyrin derivatives
34 schema:pagination 1418-1420
35 schema:productId N3928b2fc72a548cf89450b22a790dc12
36 N490b18a3c12e435090fd4a3c84d2c6b4
37 schema:sameAs https://app.dimensions.ai/details/publication/pub.1010866494
38 https://doi.org/10.1007/bf00531403
39 schema:sdDatePublished 2021-11-01T17:58
40 schema:sdLicense https://scigraph.springernature.com/explorer/license/
41 schema:sdPublisher N4d110785ac604b1fa683d90184737f01
42 schema:url https://doi.org/10.1007/bf00531403
43 sgo:license sg:explorer/license/
44 sgo:sdDataset articles
45 rdf:type schema:ScholarlyArticle
46 N09fb4daf437b4efeb8cfba62b5fd81f4 schema:issueNumber 12
47 rdf:type schema:PublicationIssue
48 N3928b2fc72a548cf89450b22a790dc12 schema:name dimensions_id
49 schema:value pub.1010866494
50 rdf:type schema:PropertyValue
51 N490b18a3c12e435090fd4a3c84d2c6b4 schema:name doi
52 schema:value 10.1007/bf00531403
53 rdf:type schema:PropertyValue
54 N4d110785ac604b1fa683d90184737f01 schema:name Springer Nature - SN SciGraph project
55 rdf:type schema:Organization
56 N656b73c1735c4e6d88dcf797935118e7 rdf:first sg:person.01070465134.19
57 rdf:rest rdf:nil
58 N9ed2ae3bf5124d4f94aaed388bf7e4f1 rdf:first sg:person.012271247736.49
59 rdf:rest N656b73c1735c4e6d88dcf797935118e7
60 Nb83273e3d4d749219a050483d0dded83 schema:volumeNumber 29
61 rdf:type schema:PublicationVolume
62 Nc57dd76277864514bbbf40d022c4ac5e rdf:first sg:person.011451527031.71
63 rdf:rest N9ed2ae3bf5124d4f94aaed388bf7e4f1
64 anzsrc-for:03 schema:inDefinedTermSet anzsrc-for:
65 schema:name Chemical Sciences
66 rdf:type schema:DefinedTerm
67 anzsrc-for:0305 schema:inDefinedTermSet anzsrc-for:
68 schema:name Organic Chemistry
69 rdf:type schema:DefinedTerm
70 sg:journal.1358699 schema:issn 0132-6244
71 1573-8353
72 schema:name Chemistry of Heterocyclic Compounds
73 schema:publisher Springer Nature
74 rdf:type schema:Periodical
75 sg:person.01070465134.19 schema:affiliation grid-institutes:grid.415738.c
76 schema:familyName Ponomarev
77 schema:givenName G. V.
78 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.01070465134.19
79 rdf:type schema:Person
80 sg:person.011451527031.71 schema:affiliation grid-institutes:grid.415738.c
81 schema:familyName Karnaukh
82 schema:givenName I. M.
83 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.011451527031.71
84 rdf:type schema:Person
85 sg:person.012271247736.49 schema:affiliation grid-institutes:grid.415738.c
86 schema:familyName Moskovskin
87 schema:givenName A. S.
88 schema:sameAs https://app.dimensions.ai/discover/publication?and_facet_researcher=ur.012271247736.49
89 rdf:type schema:Person
90 grid-institutes:grid.415738.c schema:alternateName Zashchita Specialized Center for Emergency Medical Aid, Ministry of Health of Russia, 123182, Moscow
91 schema:name Zashchita Specialized Center for Emergency Medical Aid, Ministry of Health of Russia, 123182, Moscow
92 rdf:type schema:Organization
 




Preview window. Press ESC to close (or click here)


...